蛋白酵素
抗菌肽
抗菌剂
化学
生物利用度
部分
残留物(化学)
细菌
抗生素耐药性
生物化学
生物物理学
抗生素
酶
计算生物学
肽
立体化学
生物
生物信息学
有机化学
遗传学
作者
Nils Preußke,Matthias Lipfert,Sven Rothemund,Matthias Leippe,Frank D. Sönnichsen
出处
期刊:Biochemistry
[American Chemical Society]
日期:2021-10-06
卷期号:60 (42): 3187-3199
被引量:4
标识
DOI:10.1021/acs.biochem.1c00567
摘要
α-Helical antimicrobial peptides (αAMPs) are among the potential candidates for new anti-infectives to tackle the global crisis in antibiotic resistance, but they suffer from low bioavailability due to high susceptibility to enzymatic degradation. Here, we describe a strategy to increase the resistance of αAMPs against proteases. Fusing the 12-residue αAMP KR-12 with a Trp-cage domain induces an α-helical structure in the otherwise unfolded KR-12 moiety in solution. The resulting antimicrobial Trp-cage exhibits higher proteolytic resistance due to its stable fold as evidenced by correlating sequence-resolved digest data with structural analyses. In addition, the antimicrobial Trp-cage displays increased activity against bacteria in the presence of physiologically relevant concentrations of NaCl, while the hemolytic activity remains negligible. In contrast to previous strategies, the presented approach is not reliant on artificial amino acids and is therefore applicable to biosynthetic procedures. Our study aims to improve the pharmacokinetics of αAMPs to facilitate their use as therapeutics.
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